EP1165755B1 - Banana and melon promoters for expression of transgenes in plants - Google Patents

Banana and melon promoters for expression of transgenes in plants Download PDF

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EP1165755B1
EP1165755B1 EP00918138A EP00918138A EP1165755B1 EP 1165755 B1 EP1165755 B1 EP 1165755B1 EP 00918138 A EP00918138 A EP 00918138A EP 00918138 A EP00918138 A EP 00918138A EP 1165755 B1 EP1165755 B1 EP 1165755B1
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promoter
plant
sequence
gene
gus
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EP1165755A4 (en
EP1165755A1 (en
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Stephanie K. Clendennen
Jill A. Kellogg
Chau B. Phan
Helena V. Mathews
Nancy M. Webb
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Agrigenetics Inc
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Exelixis Plant Sciences Inc
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    • C12N9/0012—Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7)
    • C12N9/0036—Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7) acting on NADH or NADPH (1.6)
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    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/415—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from plants
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    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8216—Methods for controlling, regulating or enhancing expression of transgenes in plant cells
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    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8216—Methods for controlling, regulating or enhancing expression of transgenes in plant cells
    • C12N15/8222—Developmentally regulated expression systems, tissue, organ specific, temporal or spatial regulation
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    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8216—Methods for controlling, regulating or enhancing expression of transgenes in plant cells
    • C12N15/8222—Developmentally regulated expression systems, tissue, organ specific, temporal or spatial regulation
    • C12N15/8223—Vegetative tissue-specific promoters
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    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8216—Methods for controlling, regulating or enhancing expression of transgenes in plant cells
    • C12N15/8222—Developmentally regulated expression systems, tissue, organ specific, temporal or spatial regulation
    • C12N15/823—Reproductive tissue-specific promoters
    • C12N15/8235—Fruit-specific
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    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/88—Lyases (4.)

Definitions

  • the present invention relates to novel banana fruit-associated promoters, a melon actin promoter and a banana fruit-associated/melon actin fusion promoter.
  • the invention also relates to heterologous nucleic acid constructs, vectors, kits, and transformation methods employing such promoters.
  • the invention further relates to transgenic plant cells and plants transformed with heterologous nucleic acid constructs comprising the promoters and methods for screening plant promoters in various types of plant tissue using a transient expression assay.
  • Transcriptional regulatory sequences or promoters that regulate gene expression in plants are essential elements of plant genetic engineering.
  • promoters useful for the expression of heterologous genes in plants are now available (Zhu, et al., 1995; Ni, et al., 1995).
  • Promoters for expressing a heterologous gene sequence in plants can be derived from plant DNA, e.g ., the cauliflower heat shock protein 80 (hsp 80 , Brunke and Wilson. 1993; U.S. Pat. No. 5,612,472 ), or from other sources, for example, plant viruses e.g ., the 35S cauliflower mosaic virus promoter or bacteria which infect plants, e.g ., the nopaline synthase (nos) promoter (Rogers, 1991), the octopine synthase (ocs) promoter (Leisner and Gelvin, 1988) and the mannopine synthase (mas) promoter from Agrobacterium.
  • plant viruses e.g ., the 35S cauliflower mosaic virus promoter or bacteria which infect plants, e.g ., the nopaline synthase (nos) promoter (Rogers, 1991), the octopine synthase (ocs) promoter (Leisner and Gelvin, 1988)
  • heterologous genes or selected sequences of genes in transgenic plants has typically involved the use of constitutive promoters, which drive the expression of a product throughout the plant at all times and in most tissues (e.g ., hsp80), the tomato ubiquitin promoter (Picton, et al., 1993), and the raspberry E4 promoter ( U.S. Pat. Nos. 5,783,393 ; and 5,783,394 ).
  • inducible and/or tissue specific promoters are known. Promoters that provide fruit-specific expression include the E4 and E8 promoter from tomato (Cordes, et al ., 1989: Bestwick, et al., 1995; U.S. Pat. No. 5, 859,330 ). Another fruit-specific promoter is the tomato 2A11 gene promoter. It has been demonstrated that nucleic acid sequences placed under the regulatory control of the 5' non-coding region of the tomato 2A11 gene (Van Haaren, 1993) are preferentially transcribed in developing fruit tissue. Fruit specific regulation of the kiwifruit actinidin promoter has been reported to be conserved in transgenic petunia plants (Lin, et al., 1993).
  • Pectate lyase has been previously identified as fruit- and ripening-associated in banana (Dominguez-Puigjaner et al., 1997; Medina-Suarez et al., 1997), and has recently been associated with breakdown of cell wall components and subsequent fruit softening during strawberry fruit ripening (Medina-Escobar et al., 1997).
  • Ethylene is a plant hormone influencing many aspects of plant growth and development, and is known to play a major role in the ripening process in fruits and vegetables.
  • a large amount of ethylene is also produced following trauma caused by chemicals, temperature extremes, water stress, ultraviolet light, insect damage, disease, or mechanical wounding. In some tissues, exposure to only a small amount of ethylene may cause an avalanche of ethylene production in adjacent plants or plant tissues such as fresh produce. This autocatalytic effect can be very pronounced and lead to loss of fruit quality during transportation and storage.
  • AdoMet In plants, methionine is converted to AdoMet, which is converted to ACC, which is converted to ethylene. AdoMet is synthesized via a condensation reaction between methionine and Adenosine triphosphate (ATP). A bacterial enzyme, AdoMet hydrolase (AdoMetase), which is normally not present in plant tissue, hydrolyzes AdoMet to homoserine and MTA, both of which are recycled to methionine. Plant transformation vectors, tomato fruit-specific promoters and methods of transforming plants with heterologous nucleic acid constructs effective to express AdoMetase (also termed "SAMase”) in plant cells and thereby modulate ethylene expression, have been described. See, e.g . co-owned U.S. Pat. Nos. 5,416,250 ; 5,589,623 ; 5,723,746 ; 5,750,864 ; and 5,859,330 , expressly incorporated by reference, herein.
  • TRX novel banana fruit-associated promoters designated in the present application as "TRX” and "PEL", a melon actin promoter, designated “mACTIN” and melon actin:TRX fusion promoters designated “TRX-intron” and "TRX-actin”.
  • the invention provides an isolated nucleic acid molecule comprising a banana fruit-associated TRX or "G1A" promoter.
  • the isolated nucleic acid comprises nucleotides 13 to 990 of SEQ ID NO: 1 (presented as SEQ ID NO:2), or a functional portion thereof, or is complementary to the nucleic acid sequence, and remains stably bound to it under at least moderate, and optionally, under high stringency conditions.
  • the invention provides an isolated nucleic acid molecule comprising a banana fruit-associated PEL promoter.
  • the isolated nucleic acid comprises the sequence presented as SEQ ID NO:3 ( Figures 3A and B ), or a functional portion thereof (e.g., nucleotides 564-2010 or 1099-2010 of SEQ ID NO:3), or is complementary to the nucleic acid sequence, and remains stably bound to it under at least moderate, and optionally, under high stringency conditions
  • the invention provides an isolated nucleic acid molecule comprising a melon actin promoter designated "mACTIN".
  • the isolated nucleic acid comprises the cDNA sequence presented as SEQ ID NO:4 ( Figure 4 ), or is complementary to the nucleic acid sequence, and remains stably bound to it under at least moderate, and optionally, under high stringency conditions.
  • the invention provides a TRX- monocot intron and a TRX-actin fusion promoter, designated "TRX-intron” and "TRX-actin, respectively.
  • the isolated nucleic acid comprises the TRX-intron fusion promoter sequence presented as SEQ ID NO:5 ( Figures 5A-B ), or is complementary to the nucleic acid sequence, and remains stably bound to it under at least moderate, and optionally, under high stringency conditions.
  • the isolated nucleic acid comprises the TRX-actin fusion promoter sequence presented as SEQ ID NO:6 ( Figure 6 ), or is complementary to the nucleic acid sequence, and remains stably bound to it under at least moderate, and optionally, under high stringency conditions.
  • the invention also provides nucleic acid constructs having a DNA coding sequence under the transcriptional control of a banana fruit-associated promoter, a melon actin promoter, a TRX intron fusion promoter or a banana TRX melon actin fusion promoter.
  • the DNA coding sequence is typically heterologous to the promoter and is operably linked to the promoter to enable expression of the encoded product in plant cells.
  • the banana fruit-associated, TRX-intron and TRX-actin promoters of the present invention can be used to express heterologous genes in a fruit-specific manner.
  • such promoters may be used to modulate ethylene production in transformed fruit cells and to thereby alter the ripening phenotype of transgenic fruit comprising such fruit cells.
  • the melon actin promoter of the present invention can be used to express heterologous genes in transformed plant cells, of either dicot or monocot origin.
  • the melon actin promoter can be used to consitituitively express heterologous genes in tissue of dicot or monocot plants.
  • the invention further includes a method for producing a transgenic plant such as a fruit-bearing plant.
  • a transgenic plant such as a fruit-bearing plant.
  • the chimeric gene of the present invention typically carried in an expression vector allowing selection in plant cells, is introduced into progenitor cells of selected plant. These progenitor cells are then grown to produce a transgenic plant bearing fruit.
  • the invention includes a plant cell, plant tissue, transgenic plant, fruit cell, whole fruit, seeds or calli containing any of the above-described promoters, as well as plant cells comprising the promoters and/or gene products expressed under the control of the promoters.
  • the invention provides a transient expression method for evaluating promoter expression in plant tissue.
  • a nucleic acid construct comprising a candidate promoter sequence operably linked to a GUS reporter gene is assembled, plant tissue is prepared for transformation, the nucleic acid construct is introduced into the prepared plant tissue and the plant tissue is cultured under conditions effective and for a time sufficient to detect expression of the transgene.
  • polynucleotide refers to a polymeric molecule having a backbone that supports bases capable of hydrogen bonding to typical polynucleotides, where the polymer backbone presents the bases in a manner to permit such hydrogen bonding in a sequence specific fashion between the polymeric molecule and a typical polynucleotide (e.g ., single-stranded DNA).
  • bases are typically inosine, adenosine, guanosine, cytosine, uracil and thymidine.
  • Polymeric molecules include double and single stranded ribonucleic acids (RNA) and deoxyribonucleic acids (DNA), and may include polymers having backbone modifications such methylphosphonate linkages.
  • a nucleic acid may be double stranded, single stranded, or contain portions of both double stranded and single stranded sequence.
  • the depiction of a single strand also defines the sequence of the other strand and thus also includes the complement of the sequence which is depicted.
  • nucleic acid refers to nucleic acid, originally formed in vitro, in general, by the manipulation of nucleic acid by endonucleases, in a form not normally found in nature.
  • chimeric gene construct and “chimeric nucleic acid construct” are used interchangeably and refer to recombinant nucleic acid sequences which comprise a nucleic acid coding sequence and control sequences required for expression of the coding sequence in a plant cell.
  • the term "regulatable promoter” refers to any promoter whose activity is affected by specific environmental or developmental conditions (e.g ., a tomato E4 or E8 promoter).
  • the term "constitutive promoter” refers to any promoter that directs RNA production in many or all tissues of a plant transformant at most times.
  • tissue-associated promoter refers to any promoter which directs RNA synthesis at higher levels in particular types of cells and tissues (e.g ., a fruit-associated promoter);
  • promoter or “promoter segment” refer to a sequence of DNA that functions in a promoter disclosed herein to direct transcription of a downstream gene.
  • the promoter will generally be appropriate to the host cell in which the target gene is being expressed.
  • the promoter together with other transcriptional and translational regulatory nucleic acid sequences are necessary to express a given gene.
  • control sequences also termed “control sequences”
  • the transcriptional and translational regulatory sequences include, but are not limited to, promoter sequences, ribosomal binding sites, transcriptional start and stop sequences, translational start and stop sequences, and enhancer or activator sequences.
  • plant promoter is meant a promoter or promoter region (as defined above), which in its native form, is derived from plant genomic DNA.
  • the banana fruit-associated promoters of the present invention are plant promoters.
  • a fruit-associated TRX promoter is obtained from the gene encoding a banana TRX protein, wherein the gene encoding the fruit-associated TRX protein preferably has at least about 70%, more preferably about 80%, and even more preferably about 85 to 90% sequence identity over a length of nucleic acid sequence corresponding to the banana TRX gene sequence of SEQ ID NO:1.
  • the associated fruit-associated TRX promoter is readily identified using conventional genome walking techniques (i.e ., the Universal Genome Walker Kit, Clontech Laboratories. Inc., Palo Alto, CA).
  • promoter strength refers to the level of promoter-regulated expression of a heterologous gene in a plant tissue or tissues, relative to a suitable standard (e.g., a fruit-associated promoter from a particular plant, e.g ., banana, versus a control or standard gene promoter, e.g ., the 35S CaMV promoter or the CsVMV promoter (cassava vein mosaic virus promoter, Verdaguer et al., 1998). Expression levels can be measured by linking the promoter to a suitable reporter gene such as GUS ( ⁇ -glucuronidase). Expression of the reporter gene can be easily measured by fluorometric, spectrophotometric or histochemical assays (Jefferson, et al., 1987a; Jefferson, 1987b; Jefferson, RA, 1989).
  • heterologous nucleic acid construct or sequence has a portion of the sequence which has been introduced into the plant cell in which it is expressed.
  • Heterologous, with respect to a control sequence may refer to a control sequence (i.e . promoter or enhancer) that does not function in nature to regulate the same gene the expression of which it is currently regulating.
  • heterologous nucleic acid are introduced into the cell or part of the genome in which they are present, and have been added to the cell, by transfection, microinjection, electroporation, or the like.
  • the sequences may contain a control sequence/coding sequence combination that is the same as, or different from a control sequence/coding sequence combination found in the native plant.
  • a promoter or enhancer is operably linked to a coding sequence if it affects the transcription of the sequence; or a ribosome binding site is operably linked to a coding sequence if it is positioned so as to facilitate translation.
  • operably linked means that the DNA sequences being linked are contiguous, and, in the case of a secretory leader, contiguous and in reading phase. However, enhancers do not have to be contiguous.
  • the term "gene” means the segment of DNA involved in producing a polypeptide chain, which may or may not include regions preceding and following the coding region, e.g. 5' untranslated (5' UTR) or “leader” sequences and 3' UTR or “trailer” sequences, as well as intervening sequences (introns) between individual coding segments (exons).
  • 5' UTR 5' untranslated
  • leader leader
  • 3' UTR or “trailer” sequences as well as intervening sequences (introns) between individual coding segments (exons).
  • gene may be used interchangeably herein with the term “heterologous nucleic acid coding sequence”, and the term “structural gene” means a DNA coding region.
  • sequence identity means nucleic acid or amino acid sequence identity in two or more aligned sequences, aligned using a sequence alignment program. Sequence searches are preferably carried out using the BLASTN program when evaluating the of a given nucleic acid sequence relative to nucleic acid sequences in the GenBank DNA Sequences and other public databases.
  • the BLASTX program is preferred for searching nucleic acid sequences which have been translated in all reading frames against amino acid sequences in the GenBank Protein Sequences and other public databases. Both BLASTN and BLASTX are run using default parameters of an open gap penalty of 11.0. and an extended gap penalty of 1.0, and utilize the BLOSUM-62 matrix. [See, Altschul, et al., 1997.]
  • % homology is used interchangeably herein with the term “% identity” herein and refers to the level of identity between two sequences, i.e. 70% homology means the same thing as 70% sequence identity as determined by a defined algorithm, and accordingly a homologue of a given sequence has at least about 70%, preferably about 80%, more preferably about 85%, even more preferably about 90% sequence identity over a length of the given sequence.
  • a preferred alignment of selected sequences in order to determine "% identity" between two or more sequences is performed using the CLUSTAL-W program in MacVector version 6.5, operated with default parameters, including an open gap penalty of 10.0, an extended gap penalty of 0.1, and a BLOSUM 30 similarity matrix.
  • a nucleic acid sequence is considered to be "selectively hybridizable" to a reference nucleic acid sequence if the two sequences specifically hybridize to one another under moderate stringency hybridization and wash conditions.
  • Exemplary conditions include hybridization conducted as described in the Bio-Rad Labs ZetaProbe manual (Bio-Rad Labs, Hercules. CA), expressly incorporated by reference herein. For example, hybridization is conducted in 1 mM EDTA, 0.25 M Na 2 HPO 4 and 7% SDS at 60° C, followed by washing in 1 mM EDTA, 40 mM NaPO 4 , 5% SDS, and 1 mM EDTA, 40 mM NaPO 4 , 1% SDS. Hybridization conditions are further recited in Ausubel FM et al., 1993, expressly incorporated by reference herein.
  • expression refers to the process by which a polypeptide is produced based on the nucleic acid sequence of a gene.
  • the process includes both transcription and translation.
  • transformed As used herein, the terms “transformed”, “stably transformed” or “transgenic” refer to a plant cell that has a non-native (heterologous) nucleic acid sequence integrated into its genome which is maintained through two or more generations.
  • modulate refers to a change in biological activity. Modulation may relate to an increase or a decrease in biological activity, binding characteristics, or any other biological, functional, or immunological property of the molecule.
  • ethylene regulated refers to regulation which is induced by changes in ethylene concentration in the plant.
  • promoter activity which occurs or primarily occurs, during later stages of fruit development and/or early stages of fruit ripening, is said to be ethylene regulated.
  • a "plant cell” refers to any cell derived from a plant, including undifferentiated tissue (e.g ., callus) as well as plant seeds, pollen, progagules and embryos.
  • G1A One of the fragments, G1A, was hybridized to RNA from banana pulp at different stages of ripening.
  • the G1A transcript was found to increase with fruit ripening.
  • G1A was found to be represented by a small gene family in banana.
  • the recovered differential display product was used as a probe on Northern blots to confirm tissue distribution of the associated transcript.
  • Results from Northern blot analysis using G1A as a probe indicate that the native transcript is approximately 600nt, and highly fruit-associated (not detected in any other tissue analyzed including root, corm, leaf, or in vitro plantlet).
  • G1A transcript was hybridized to RNA from banana pulp at different stages of ripening, it was barely detectable in green bananas not treated with ethylene, and the transcript abundance increased dramatically after ethylene treatment and during ripening.
  • differential display products were sequenced and compared to sequences available in GenBank, using a basic BLASTN search of non-redundant nucleic acid sequence databases through NCBI (http://www.ncbi.nlm.nih.gov/index.html), using default parameters and G1A (TRX) was found to display significant sequence similarity to other plant thioredoxin genes.
  • TRX The sequences for many plant thioredoxin genes were found in GenBank.
  • the coding sequence of banana G1A, designated herein as TRX, is 58.6% (280 out of 478 nucleotides) identical at the nucleotide level to its closest neighbor, wheat thioredoxin (TRX). Accession AJ009762. Outside of the coding sequence, which includes the TRX promoter, no significant matches between the banana sequence and any other sequence in GenBank was detected using the BLASTN program with default parameters.
  • Thioredoxin is known to exist in higher plants in several forms.
  • the m and f isoforms are chloroplastic, whereas the h isoform is cytosolic and lacks both a signal and transit sequence.
  • Two wheat thioredoxin genes have recently been characterized and appear to contain a transmembrane domain at the N-terminus, indicating a membrane association.
  • the coding sequence associated with the banana thioredoxin described herein is most similar to the h isoform, and lacks any apparent presequence, suggesting that it cytosolic.
  • Thioredoxin h genes generally exist as small gene families in higher plants, although at least five putative sequences have been characterized in Arabidopsis. Both wheat and tobacco have two closely related thioredoxin h genes that are differentially expressed. Prior to the present invention, a fruit-associated thioredoxin had not been reported.
  • Upstream sequences associated with the TRX banana differential display product were isolated in a series of steps, as detailed in Example 1.
  • the upstream sequences were isolated by genome walking an assembled into a contiguous sequence ( Figures 1A-D ).
  • a modified promoter sequence, with restriction sites engineered into the 5' and 3' ends was constructed for incorporation into the pAG 159 reporter gene construct, as described below in Example 1.
  • Pectate lyase was previously associated with fruit and ripening in banana (Dominguez-Puigjaner et al., 1997; Medina-Suarez et al., 1997), and with the breakdown of cell wall components and subsequent fruit softening during strawberry fruit ripening (Medina-Escobar et al., 1997).
  • Two banana and one strawberry pectate lyase cDNA sequences may be found in GenBank at Accession numbers X92943, Z93106 and U63550, for PEL1, PEL2 and strawberry PEL, respectively.
  • pectate lyase in banana fruit is coordinated with ripening and can be stimulated by exogenous ethylene (Dominguez-Puigjaner et al, 1997.)
  • tissue distribution of the PEL transcript has not been previously reported.
  • PCR amplification of banana genomic DNA with oligonucleotide primers complimentary to conserved regions of the PEL coding sequence yielded two different-sized products (PEL1 and PEL2), which were cloned, sequenced, and used to design gene-specific oligonucleotide primers.
  • PEL1 and PEL2 two different-sized products
  • RT-PCR reverse transcriptase polymerase chain reaction
  • a cDNA library was generated and adaptors ligated to double-stranded cDNA in order to provide a PCR-accessible library for rapid amplification of cDNA 5' or 3' ends (5' or 3' RACE, respectively), as detailed in Example 2, below.
  • a putative promoter fragment of approximately 2.5 kb was amplified from the ScaI digested genomic banana library, cloned and completely sequenced.
  • the PEL1 2.5kb promoter fragment was subcloned as a translational fusion with GUS in a reporter gene construct, then truncated at the 5' end to generate promoter fragments 2.0 kb (SEQ ID NO:3) and truncations thereof 1.4 kb, and 0.9 kb as described in Example 2. See, also Figs. 3A and 3B .
  • the various PEL promoter fragments were incorporated into reporter constructs in translational fusion with a GUS sequence, also described in Example 2.
  • Actin is a ubiquitously expressed protein that is an integral component of the cytoskeleton. Because of its high degree of conservation and abundant expression in almost every eukaryotic tissue, actin has become a common standard or control gene in the study of biological systems. Actin expression is generally considered to be both ubiquitous and constitutive and actin sequences and gene structure are well-conserved among plants. In plants, functional actin genes are commonly comprised of five exons interrupted by four introns. The intron positions are well conserved among plants and are rather small, although the intron length and sequence are variable. See, e.g ., Pearson and Meagher, 1990, soybean actin: An et al. , 1996, Arabidopsis actin: and McElroy et al., 1990, rice.
  • mACTIN melon actin promoter
  • SEQ ID NO:4 The mACTIN promoter sequence (SEQ ID NO:4) is derived from a dicot, however, it exhibits surprisingly strong constitutive promoter activity in both monocots and dicots. Although the promoter is of plant origin, it exhibits a level of promoter activity that is similar to the commonly used CaMV viral promoter.
  • the banana fruit-specific TRX promoter exhibited a moderate level of activity as determined by transient reporter gene activity in banana fruit slices.
  • Two modified forms of the promoter were constructed by (1) adding a monocot intron to the 3' end of the banana TRX promoter and (2) by fusing the banana TRX promoter with the melon actin promoter at the TATA-box.
  • the melon actin promoter is a strong constitutive promoter that is active in both monocots and dicots and does contain an intron in the 5' untranslated leader. While the mechanism is not part of the invention, it was predicted that the addition of an intron in the 5' untranslated leader to the banana TRX promoter would increase the activity of the banana TRX promoter, but that the fruit-specificity of the TRX promoter would remain unchanged since the functional elements controlling tissue specificity are predicted to occur upstream of the TATA-box.
  • Example 4 The construction and evaluation of a TRX-melon actin and a TRX-monocot intron fusion promoter is further described in Example 4. According to the results of transient expression assays using the modified TRX promoters, the fusion promoters demonstrate improved performance relative to the banana fruit-specific TRX promoter in transient expression assays.
  • the present invention provides vectors suitable for the transformation of plants.
  • the vectors, chimeric genes and DNA constructs of the present invention are also useful for the expression of heterologous genes.
  • Transgenic plants, transgenic plant cells and transgenic fruit, carrying the chimeric genes of the present invention may be a useful source of recombinantly-expressed material.
  • the banana fruit-associated and TRX fusion promoters of the invention find utility in chimeric gene constructs for the fruit-associated expression of heterologous structural genes operably linked to a promoter.
  • the methods and results described herein are directed to fruit-associated gene expression under the control of the banana fruit-associated and TRX fusion promoters of the invention, as well as consitituitive gene expression under the control of the melon actin promoter in transgenic plant cells.
  • the promoters of the invention include a region of DNA that promotes transcription of a gene operably linked thereto, in transformed plant cells.
  • heterologous gene constructs can be made whereby a foreign structural DNA sequence of interest, or gene, can be placed under the regulatory control of a banana fruit-associated promoter of the invention.
  • the expression vectors of the invention may be constructed to containing an insertion site for a DNA coding sequence of interest. The transcription of such inserted DNA is then under the control of a banana fruit-associated promoter of the invention.
  • Such expression vectors may have single or multiple transcription termination signals at the 3' end of the DNA sequence being expressed.
  • the expression cassette may also include, for example, (i) a DNA sequences encoding a leader sequence (e.g ., to allow secretion or vacuolar targeting), (ii) translation termination signals, (iii) selectable marker genes for use in plant cells. (iv) sequences that allow for selection and propagation in a secondary host, such as an origin of replication and a selectable marker sequence.
  • Selectable marker genes encode a polypeptide that permits selection of transformed plant cells containing the gene by rendering the cells resistant to an amount of an antibiotic that would be toxic to non-transformed plant cells.
  • exemplary selectable marker genes include the neomycin phosphotransferase ( npt II) resistance gene, hygromycin phosphotransferase ( hpt ), bromoxynil-specific nitrilase ( bxn ), phosphinothricin acetyltransferase enzyme (BAR) and the spectinomycin resistance gene ( spt ), wherein the selective agent is kanamycin, hygromycin, geneticin, the herbicide glufosinate-ammonium (“Basta”) or spectinomycin, respectively.
  • Typical secondary hosts include bacteria and yeast.
  • the secondary host is Escherichia coli
  • the origin of replication is a colE1-type
  • the selectable marker is a gene encoding ampicillin resistance.
  • Origin of replication and selectable marker sequences operative in secondary hosts are well known in the art and many are commercially available ( e.g., Clontech. Palo Alto, CA; Stratagene, La Jolla, CA).
  • the vectors of the present invention are useful for fruit tissue-associated expression (using a banana TRX or PEL promoter, a TRX-intron or a TRX actin fusion promoter) or constituitive expression (mACTIN) of nucleic acid coding sequences in plant cells.
  • a selected peptide or polypeptide coding sequence can be inserted in an expression vector of the present invention.
  • the vector is then transformed into host cells, and the host cells cultured under conditions to allow the expression of the protein coding sequence.
  • the expressed peptide or polypeptide is isolated from the cells.
  • Transformed plant progenitor cells can also be used to produce transgenic plants bearing fruit.
  • the invention includes a method for producing a transgenic fruit-bearing plant, where fruit produced by the plant has a modified phenotype.
  • a heterologous gene construct is introduced ( e.g ., by transformation) into progenitor cells of the plant.
  • An exemplary heterologous gene construct is composed of (i) a DNA sequence encoding a gene product effective to modify a phenotypic characteristic of the plant, e.g ., to reduce ethylene biosynthesis in fruit produced by the plant, operably linked to (ii) a banana or TRX fusion promoter of the invention wherein expression is fruit-associated.
  • the invention includes a method for producing a transgenic plant, where an exemplary heterologous gene construct is composed of (i) a DNA sequence encoding a transgene product, operably linked to (ii) a melon actin promoter wherein expression is constituitive.
  • the DNA sequence is heterologous to the promoter and the chimeric gene contains the appropriate regulatory elements necessary for expression in a plant cell.
  • Transformed progenitor are grown to produce a transgenic plant bearing fruit.
  • the method further includes transforming progenitor cells of the plant with a vector containing a selectable marker and the heterologous gene.
  • vectors described herein may form part of a plant transformation kit.
  • Other components of the kit may include, but are not limited to, reagents useful for plant cell transformation.
  • Chimeric genes containing a banana fruit-associated promoter of the invention e.g. , TRX or PEL.
  • a melon actin promoter of the invention, a TRX:intron or a TRX:melon actin fusion promoter of the invention can be transferred to plant cells by any of a number of plant transformation methodologies, including Agrobacterium- based methods [Ranier et al., 1990 (rice). McCormick et al., 1986 (tomato): Norelli et al., 1996 (apple)], electroporation, microinjection, and microprojectile bombardment. (See, e.g ., Comai and Coning. 1993; Klein, et al., 1988; Miki, et al. 1987; Bellini. et al., 1989).
  • chimeric genes are introduced into plants by way of a T-DNA-less Ti plasmid carried by Agrobacterium tumefaciens, followed by co-cultivation of the A. tumefaciens cells with plant cells.
  • vectors for use in the invention contain a selectable marker gene, T-DNA border regions from Agrobacterium tumefaciens, a heterologous gene of interest, and other elements as desired.
  • Exemplary Agrobacterium transformation vectors are commercially available from Clontech (Palo Alto, CA) and further described by An, et al. , 1985.
  • suitable vectors may be constructed using the promoters of the present invention and standard plant transformation vectors, which are available both commercially (Clontech, Palo Alto, CA) and from academic sources [Salk Institute, Plant Biology Labs; Texas A & M University (Frisch et al., 1995); Waksman Institute, Rutgers, The State University of New Jersey, Piscataway, NJ].
  • Another embodiment is based on microprojectile bombardment using microparticles loaded with DNA which are bombarded into the cells using "gene gun” technology. (See, e.g ., Robinson, HL and Torres, CA, 1997.)
  • the transformation vector When electroporation or microprojectile bombardment transformation techniques are utilized, the transformation vector generally contains the heterologous gene of interest and a selectable marker gene construct to determine whether the transformation event was successful.
  • Transformed plant cells are obtained as a result of the transformation of the plant cells with a heterologous gene construct containing a promoter of the invention operably linked to a heterologous gene.
  • the plant cells are cultured in medium containing the appropriate selection agent to identify and select for plant cells which express the chimeric gene. After plant cells that express the chimeric gene are selected, whole plants are regenerated from the transgenic plant cells. Techniques for regenerating whole plants from transformed plant cells are known in the art. Suitable plant regeneration protocols are also known.
  • the invention further includes a method for producing a transgenic plant such as a fruit-bearing plant.
  • a transgenic plant such as a fruit-bearing plant.
  • the chimeric gene of the present invention typically carried in an expression vector allowing for selection in plant cells, is introduced into progenitor cells of a plant. These progenitor cells are then grown to produce a transgenic plant bearing fruit.
  • Preferred plants suitable for transformation using the banana fruit-associated, melon actin and TRX fusion promoters of the invention include but are not limited to, banana, tomato, pineapple, grape, raspberry, strawberry, kiwi fruit, avocado, melon, mango, papaya, apple, peach, pear, cherry, citrus, date palm, plantain, soybean, cotton, alfalfa, oilseed rape, flax, sugar beet, sunflower, potato, tobacco, maize, wheat, rice, nuts and lettuce.
  • cotyledon explants of a commercial cantaloupe variety are transformed according to known methods (Fang and Grumet. 1990; Valles and Lasa. 1994: Dong, et al., 1991; Gonsalves, et al., 1994, Yoshioka, et al., 1992; Ayub, et al., 1996), using the a disarmed Agrobacterium strain to introduce the above-described binary vectors into plants.
  • the disarmed Agrobacterium strain is co-cultivated with melon cotyledon tissue explants, and primary transformants selected on the basis of their capacity to regenerate and develop roots on media containing the antibiotic, kanamycin.
  • Agrobacterium transformation methods as described for banana, rice, tomato, apple are used to transform plant cells using a promoter of the invention.
  • Agrobacterium transformation has been previously described for rice, tomato, apple, almond, asparagus, avocado, broccoli, carrot, cauliflower, celery, cucumber, grape, persimmon, and spinach.
  • Any structural gene of interest may be placed under the regulatory control of a promoter of the invention.
  • the structural gene may encode for a polypeptide of interest or other gene product.
  • heterologous genes may be operably linked to a banana fruit-associated, melon actin or TRX fusion promoter of the invention.
  • banana fruit-associated promoters of the invention are used to modulate ethylene production in transformed fruit cells, and thereby alter the ripening and delay senescence of transgenic fruit composed of such fruit cells.
  • the promoters described herein are employed in a method for prolonging ripening and delaying senescence of fruit from a fruit-bearing plant, e.g., banana.
  • transgenic plant cells containing the promoters of the present invention are grown to produce a transgenic plant bearing fruit.
  • plant cells are transformed with a heterologous nucleic acid construct encoding a product capable of reducing ethylene biosynthesis when expressed in plant cells (e.g ., S-adenosyl-methionine hydrolase (SAMase, Ferro et al., 1995: Hughes et al., 1987), aminocyclopropane-1-carboxylic acid (ACC) deaminase, ACC oxidase antisense molecule, ACC synthase antisense molecule, ACC oxidase cosuppression molecule, ACC synthase cosuppression molecule), which is under the control of a banana promoter of the invention.
  • SAMase S-adenosyl-methionine hydrolase
  • ACC aminocyclopropane-1-carboxylic acid
  • a modified ripening phenotype refers to an alteration in the rate of ripening; characterized by an increased ripening time course, or prolonged ripening and the delayed senescence of, a transgenic fruit relative to corresponding (i. e. , non-transgenic) wild-type fruit.
  • the nucleic acid coding sequence can correspond to a pathogenesis related gene, such as polygalacturonase inhibiting protein (PGIP), glucanase and chitinase.
  • PGIP polygalacturonase inhibiting protein
  • glucanase glucanase
  • chitinase a pathogenesis related gene
  • the nucleic acid coding sequence includes sequences which affect: (i) flavor (e.g ., thaumatin; GenBank); (ii) pigmentation (e.g ., products that modify lycopene synthesis, such as lycopene cyclase; GenBank); (iii) enzymes or other catalytic products (such as, ribozymes or catalytic antibodies) that modify plant cell processes; (iv) enzymes that inhibit degradation of ripened fruit (e.g ., antisense polyphenol oxidase and antisense polyphenol peroxidase (to inhibit browning) and antisense pectate lyase (to inhibit softening); (vi) antimicrobial peptides, (vii) sucrose accumulating genes, such as the sucrose phosphate synthase gene (GENBANK) and (viii) genes which affect the metabolism of sucrose (e.g ., invertase).
  • flavor e.g thaumatin; Gen
  • transgenic plant cells are assayed for expression of a transgene which is operably linked to a banana fruit-associated, melon actin or TRX fusion promoter of the invention.
  • Transgenic plant cells may be initially selected by their ability to grow in the presence of a selective agent, such as the aminoglycoside antibiotic, kanamycin,
  • Expression of a transgene may also be determined by analysis of DNA, mRNA, and protein, associated with the expression of the transgene.
  • the assays are typically conducted using various plant tissue sources, e.g ., leaves, stem, or fruit.
  • the relative activity of the banana fruit-associated promoters of the invention was evaluated in a transient assay system using a reporter gene, exemplified by GUS d( ⁇ -glucuronidase), effective to evaluate the tissue-associated regulatable expression from the promoters
  • GUS d( ⁇ -glucuronidase) a reporter gene, exemplified by GUS d( ⁇ -glucuronidase)
  • Expression of GUS protein is easily measured by fluorometric, spectrophotometric or histochemical assays (Jefferson, 1987a).
  • Recombinant nucleic acid constructs comprising; pAG142a-pel::GUS (2.0kb), pAG142b-pel::GUS (1.4kb), pAG142c-pel::GUS (0.9kb), pAG153-CsVMV::GUS, pAG159-TRX::GUS and pBI221-35S::GUS were prepared using the isolated promoter sequences and techniques routinely employed by those in the art, then introduced into banana plant cells by particle bombardment, as described below in Examples 1 and 2.
  • FIG. 7 illustrates the results of GUS reporter assays with the pAG142a-pel::GUS (PEL 2.0), pAG142b-pel:: GUS (PEL 1.4), pAG142c-pel:: GUS (PEL 0.9), pAG153-CsVMV::GUS (CsVMV), and pAG159-TRX::GUS (TRX 1.0) promoters in edible banana pulp (external surface of the pulp in contact with the peel) at green, peel color index (PCI) 1 (early) and PCI 4 (later) stages of ripening. The results are reported as the percent of banana fruit slices with GUS foci.
  • PCI peel color index
  • the relative activity of the melon actin, TRX-intron and TRX-actin fusion promoters of the invention was evaluated in a transient assay system using a GUS ( ⁇ -glucuronidase) reporter gene, as described above.
  • the melon actin promoter was evaluated together with various control promoters in both garlic and onion and the negative control (promoterless GUS) showed no foci, whereas the pAG138m-RE4::GUS; pAG153-CsVMV:: pAG167-mACTIN::GUS; and PBI221-35S::GUS (CaMV 35S) all promoted GUS expression, as detailed in Example 3 .
  • TRX-intron and TRX-actin modifications resulted in improved performance relative to the banana fruit-specific TRX promoter. More specifically, the TRX-actin fusion promoter displays transient expression activity approximately equal to the strong constitutive promoter CsVMV, whereas the TRX-intron fusion is slightly less active on average. Furthermore, the TRX-intron and TRX-actin promoters have lower activity in banana leaves, indicating that the promoters have retained the tissue specificity of the TRX promoter (Example 4).
  • the mACTIN promoter was also tested for activity in a model dicot ( Arabidopsis thaliana ) after transformation with a nucleic acid construct containing the reporter gene encoding GUS under the control of the mACTIN promoter.
  • Plasmid pAG4015 which contains two expression cassettes: (1) adjacent to the left T-DNA border is found the selection cassette containing the nptII gene conferring kanamycin resistance under the control of the CsVMV promoter together with the G7 terminator; and (2) adjacent to the right T-DNA border is found the GUS reporter gene under the control of the mACTIN promoter together with the nos terminator.
  • Arabidopsis thaliana plants were transformed with pAG4015 by in planta Agrobacterium-mediated transformation, T1 seed was harvested from the plants, germinated and transformed seedlings identified based on kanamycin resistance, as further described in Example 3.
  • Transgenic plants may be assayed for their ability to synthesize product mRNA, DNA, protein, and/or for their resistance to an antibiotic, e.g ., the aminoglycoside antibiotic, kanamycin.
  • the assays are typically conducted using various plant tissue sources, e.g ., leaves, stem, or fruit
  • Gene amplification and/or expression may be measured in a sample directly, for example, by conventional Southern blotting, Northern blotting to quantitate the transcription of mRNA [Thomas, 1980), dot blotting (DNA analysis), or in situ hybridization, using an appropriately labeled probe, based on the sequence or the transgene being expressed under the control of the various promoters described herein.
  • banana fruit-specific promoters described herein include the fruit specific expression of genes that may alter or improve characteristics of the fruit. Of particular interest are ripening control, modification of the nutritional content of fruit, and expression of useful proteins in a fruit-specific manner.
  • the melon actin promoter described herein is useful for controlling expression of selectable markers and for constitutive expression of genes of interest. It functions in both monocots and dicots and has activity similar to a commonly used viral promoter, but it is of plant origin.
  • the melon-actin fusion promoters described herein have similar properties, however, in addition they have retained the tissue specificity of the banana TRX promoter.
  • Biological reagents were typically obtained from the following vendors: 5' to 3' Prime, Boulder. CO: New England Biolabs. Beverly, MA: Gibco/BRL, Gaithersburg. MD: Promega, Madison. WI: Clontech. Palo Alto, CA; and Operon, Alameda, CA.
  • Specific reagents employed in the particle bombardment include BioRad Biolistic PDS-1000/He system (BioRad Laboratories, Hercules, CA, USA), gold particles of 1.5 - 3.0 ⁇ m (Aldrich. Milwaukee. WI, USA), a rupture disk: 1,100 PSI (BioRad Laboratories, Hercules, CA. USA), stop screens of 0.685 mesh (Rumsey-Loomis, Freeville, NY), macrocarriers: (Rumsey-Loomis, Freeville, NY) and X-Gluc: 5-Bromo-4-chloro-3-indoyl ⁇ -D-glucuronide cyclohexylamine salt (Rose Scientific, Edmonton, Alberta, Canada).
  • Specific equipment and reagents employed in particle bombardment include BioRad Biolistic PDS-1000/He system (BioRad Laboratories, Hercules, CA, USA), gold particles of 1.5 - 3.0 ⁇ m (Aldrich, Milwaukee. WI.
  • a rupture disk 1, 100 PSI (BioRad Laboratories, Hercules, CA, USA), stop screens of 0.685 mesh (Rumsey-Loomis, Freeville, NY), macrocarriers: (Rumsey-Loomis, Freeville, NY) and X-Gluc: 5-Bromo-4-chloro-3-indoyl ⁇ -D-glucuronide cyclohexylamine salt (Rose Scientific, Edmonton, Alberta, Canada).
  • Solutions for use in GUS assays included: 50% Glycerol (vol/vol); 2.5M calcium chloride (CaCl 2 . 13.875 grams anhydrous CaCl 2 dissolved in 50 mls sterile diH 2 O); 0.1M spermidine (0.1452 grams dissolved in 10 mls sterile diH 2 O); 70% EtOH (vol/vol), 3 mls sterile diH 2 O in 7 mls 200 proof ethyl alcohol; X-gluc solution (200 ml prepared by adding the components in the amounts shown in Table 1, below, to 198 ml distilled H 2 O, stirring for 10 minutes or until dissolved, adjusting the pH to 7.0.
  • Gold particle suspensions are prepared by adding 30 ⁇ l of gold particles (1.5 ⁇ m to 3.0 ⁇ m) to a high quality microcentrifuge tube followed by addition of 1 ml 70% EtOH. The suspension is vortexed for 20 seconds and left to stand for 25 minutes, allowing the particles to settle to the bottom of the tube so that they do not stick to the side of the tube when centrifuging, followed by centrifuging in a microcentrifuge for 6 minutes at 13,000 rpm. The supernatant is carefully removed, discarded and 500 ⁇ l sterile diH 2 O added to the tube which is vortexed for 10 seconds and left standing for 25 additional minutes, followed by centrifuging in a microcentrifuge for 6 minutes at 13,000 rpm. The supernatant is carefully removed, discarded, 500 ⁇ l sterile 50% glycerol stock added and the mixture vortexed until the particles are resuspended.
  • DNA solutions containing the GUS recombinant nucleic acid constructs were prepared by adding 50 ⁇ l (1 ⁇ g/ ⁇ l) DNA to a microcentrifuge tube containing the gold and gently vortexing for 2-3 seconds, followed by adding 500 ⁇ l cold CaCl 2 (2.5M) and gently vortexing for 2-3 seconds, adding 200 ⁇ l cold spermidine (0.1M) and gently vortexing at low speed at 4°C, tapping the tube a couple of times every 5-10 minutes to make sure particles remained suspended, with a total vortex time of about 40 minutes.
  • the centrifuge tube was pulsed to a maximum of 1,500 rpm in a microcentrifuge at 4°C three times, the supernatant removed and discarded.
  • Banana fruit was prepared for particle bombardment by wiping with a towel soaked in 95% ethyl alcohol, trimming off the pedicel stalk and the tip of the fruit, and placing in a beaker.
  • An amount of a water/soap mix (4 drops antimicrobial soap/1000 ml H 2 O) sufficient to cover the fruit was added and shaken intermittently for 15 minutes, then rinsed with diH 2 O, until the soap was gone.
  • An amount of 75 % EtOH sufficient to cover the fruit was added and shaken gently each minute for 4 minutes, the EtOH was drained off and an amount of 10% bleach/2 drops Tween 20/1000 ml sufficient to cover the fruit was added and shaken intermittently for 10 minutes.
  • the bleach was drained off and the fruit rinsed 3 times with sterile diH 2 O, followed by rinsing once with sterile 500 ml diH 2 O/2 ml PPM mix (Plant Preservative Mixture, Plant Cell Technology, Washington, DC), and soaking in media consisting filter sterilized 200 mg/l ascorbic acid and 200 mg/l citric acid, until ready to be cut. Before cutting, the fruit was blotted dry on filter paper.
  • Ungassed green banana fruit, gassed banana fruit just before softening stage (not quite yellow) and gassed banana fruit 24 hours after gassing were generally used in transient assays.
  • the types of tissue used included, longitudinal slices of the outside of the fruit pulp without peel (the portion that touches peel), segments of the inside of the peel, segments of the outside of the peel, cross sectional slices including the peel and longitudinal slices of the seed region (middle portion of the fruit).
  • PAC1 medium which contains: MS salts, B5 vitamins, glycine 2 mg/l, sucrose 3%, casein hydrolysate 100 mug/l, BA 0.5 mg/l, 2,4-D 1.5 mg/l, PPM 5 ml/l, ascorbic acid 100 mg/l, citric acid 100 mg/l, cefotaxime 200 mg/l (aa) pH 5.8 and Phytagel 0.25.
  • the transient assay is based on particle bombardment of plant tissue sections with a suspension of DNA and gold particles as described above.
  • the fruit tissue was bombarded using GUS reporter constructs, a flight distance of 6 cm and a PSI of 1,100. Flight distance is defined as the distance between the DNA coated microcarrier and stopping screen to the target cells.
  • PSI refers to the helium pressure in the gas acceleration tube used for particle bombardment.
  • RNAimage ® Kits [Cat. No.: G501-G510], GenHunter Corporation, 624 Grassmere Park Drive, Suite 17 / Nashville, TN 37211 / USA, Tel: 615-833-0665 / Fax: 615-832-9461, genhunt@telalink.net http://www.nashville.net/ ⁇ genhunt/ kimage. html].
  • First-strand cDNA was synthesized from 50 ⁇ g DNase-treated total RNA using single-base anchored oligo(dT) primers containing a HindIII restriction site (H-T 11 G, SEQ ID NO:15; H-T 11 A, SEQ ID NO:16; and H-T 11 C, SEQ ID NO:17).
  • the cDNA was then amplified in duplicate in the presence of a radiolabeled nucleotide (in this case, ⁇ -[33P] dATP), and the resulting products analyzed on a denaturing polyacrylamide gel. Products specific to a certain tissue were identified after separation and autoradiography. After desired amplification products were identified, they were recovered directly from the dried acrylamide gel, re-amplified with the original primer set, then further characterized.
  • a radiolabeled nucleotide in this case, ⁇ -[33P] dATP
  • Amplification products associated with ripe banana pulp were recovered from acrylamide gels, re-amplified with the original primer set, and the differential display products used as probes on Northern blots to confirm tissue distribution of the associated transcript.
  • Results from Northern blot analysis using G1A (TRX) as a probe indicate that the native transcript is approximately 600 nucleotides long and highly fruit-associated.
  • Upstream sequences associated with the banana differential display product TRX were isolated in a series of steps.
  • the first oligonucleotide primer was designed complementary to the 5' end of the differential display fragment and used to walk upstream in a PCR-accessible banana genomic library (Universal Genome Walker Kit, catalog #K1807, Clontech Laboratories, Inc., 1020 East Meadow Circle, Palo Alto, CA 94303-4230).
  • PCR-accessible banana genomic libraries were constructed and screened according to the supplier's protocol, using the five restriction endonucleases included in the kit ( Eco RV, Sca I, Dra I, Pvu II, and Ssp I), and three additional blunt-cutters which were used to digest genomic DNA prior to adaptor ligation: HpaI, MscI, and PshAI. After two rounds of amplification of the banana libraries using thrdx 3'R (SEQ ID NO:18) and H-AP1 (SEQ ID NO:7, GenHunter Corp..
  • fragments each consisted of a partial intron I, followed by exon II and intron II and a partial exon III.
  • the nucleotide sequence of exon II and the partial exon III was identical between fragments #13 and #14. However, sequence differences in the introns were apparent.
  • fragment #13 the predicted intron II size is 90bp, while the predicted intron size in fragment #14 is 96 bp, due to a 6 nucleotide insertion.
  • trx 3'R-2 SEQ ID NO:19
  • trx 3'R-3 SEQ ID NO:20
  • a 1.2 kb fragment was amplified from the PshAI library.
  • the fragment contained the rest of intron I, the complete exon I, and upstream sequence, including a putative TATA-box.
  • the nucleotide sequence of this 1.2kb fragment was identical to the intron I sequence of fragment #14 described previously.
  • a 5'RACE product was amplified from a PCR-accessible cDNA library made from banana pulp (PCI 4) RNA (Marathon cDNA Amplification Kit, Clontech) using the thrdx3'R primer (SEQ ID NO:18).
  • the 300 bp product matched the sequence of the exons in the 1.2 kb fragment, which in turn was contiguous with fragment #14.
  • TRX14A SEQ ID NO: 23
  • TRX14B SEQ ID NO:24
  • SEQ ID NO:1 The entire nucleotide sequence of the banana TRX gene is shown in Figure 1 (SEQ ID NO:1), which depicts the complete annotated nucleotide sequence, including the coding sequence and intron(s). Nucleotides 13 through 990 of SEQ ID NO:1 correspond to the banana fruit-associated TRX promoter of the invention, presented herein as SEQ ID NO:2.
  • Restriction sites were engineered into the primers used to amplify the TRX promoter directly from banana genomic DNA in order to clone the sequence.
  • a BamHI site and NcoI site were engineered into the 5' and 3' primers, TRXP-F (SEQ ID NO:25) and TRXP-R (SEQ ID NO:26), respectively, in order to incorporate cloning sites for use in preparation of recombinant nucleic acid constructs, as further described below.
  • TRXP-F SEQ ID NO:25
  • TRXP-R SEQ ID NO:26
  • the nucleotide sequence of the TRX promoter, as it exists in pAG159, is presented in SEQ ID NO:2 ( Figure 2 ).
  • the TRX promoter sequence in pAG 159 differs from the nucleotide sequence assembled from genomic amplifications ( Figure 1 ) in that a BamHI site (GGATCC) and an NcoI site (CCATGG) have been engineered into the 3' and 5' ends of the sequence, respectively.
  • the translational start codon consists of the ATG contained within the 3' NcoI site.
  • the sequence in Figure 2 (SEQ ID NO:2) has been shown to encode a functional promoter.
  • pAG159-TRX::GUS pAG142a-pel::GUS (2.0kb)
  • pAG142b-pel::GUS 1.4kb
  • pAG142c-pel::GUS 0.kb
  • pAG153-CsVMV::GUS and pBI221-35S::GUS recombinant nucleic acid constructs were individually introduced into banana tissue by particle bombardment.
  • the pBI221-35S::GUS and pAG153- CsVMV:GUS constructs contain the CaMV 35S and CsVMV promoters, respectively, which drive GUS expression. Both are strong constitutive promoters which serve as positive controls for expression.
  • the relative activity of the banana fruit-associated promoters was determined by transient assay system using the GUS reporter gene.
  • the transient assay is based on particle bombardment of plant tissue sections with a suspension of DNA and gold particles as described above.
  • a cDNA library was generated using RNA isolated from ripening banana pulp. Total banana RNA was extracted from banana pulp tissue (PCI 4) using the protocol in Clendennen and May, 1997, and poly(A)+ RNA was isolated from 17 ⁇ g DNase-treated total RNA using the Straight A's mRNA Isolation System Kit [Novagen, Inc., Madison, Wisconsin]. The library was made using Clontech's Marathon cDNA Amplification Kit [Clontech Laboratories, Inc.: Marathon cDNA Amplification Kit, Palo Alto, California 94303-4230], following the manufacturer's protocol. Briefly, after first and second-strand cDNA synthesis, adaptors were ligated to the polished ends of the double-stranded cDNA. This cDNA library served as a PCR-accessible library for rapid amplification of cDNA 5' or 3' ends.
  • a rapid amplification of cDNA 5' ends (5' RACE) reaction was performed with adaptor-specific and PEL1 gene-specific (PEL 3'R-2, SEQ ID NO:27) oligonucleotide primers.
  • the 5' end of the banana PEL1 cDNA was amplified using the manufacturer's suggested conditions for RACE amplifications (Clontech).
  • a 5' RACE product of approximately 900 bp was isolated, cloned, and sequenced.
  • a putative translational start site was identified and gene-specific oligonucleotides were designed to walk upstream in a banana genomic library.
  • the pectate lyase (PEL) fruit-associated promoter was isolated in a series of steps.
  • a PCR-accessible genomic library was made from banana genomic DNA using the Clontech Universal GenomeWalker Kit [Clontech Laboratories, Inc, Palo Alto, California]. Following the suggested protocol from the manufacturer, five blunt-cutter restriction enzymes were used separately to digest genomic banana DNA: DraI, EcoRV, PvuII, ScaI, and StuI. Once purified, the digested DNA fragments were ligated to adaptor ends supplied in the kit. This served as a PCR-accessible library for amplification of genomic sequence upstream of the PEL1 start codon.
  • PFBAN3'R, SEQ ID NO:28, and PF Pec 3'R, SEQ ID NO:29 Two gene-specific oligonucleotides (PFBAN3'R, SEQ ID NO:28, and PF Pec 3'R, SEQ ID NO:29), were used in nested primer reactions, and a putative promoter fragment of approximately 2.5 kb was amplified from the ScaI digested genomic banana library. The fragment was cloned and completely sequenced.
  • the PEL1 2.5kb promoter fragment was subcloned as a translational fusion with GUS in a reporter gene construct. It was engineered with a 5' end PstI site and 3' end SnaBI site. In addition to assaying promoter function of the 2.5kb PEL1 promoter fragment, a series of 5' deletions was generated from the 2.5kb PEL1 upstream sequence. The PEL1 deletions were made by restricting the cloned fragment with Sph1 and Spel restriction enzymes, leaving intact a 5'overhang susceptible to enzymatic digestion by E . coli exonuclease III [New England Biolabs, Beverly, MA].
  • Truncated PEL1 promoter fragments of 2.0, 1.4, and 0.9kb in a translational fusion with GUS were generated by this method.
  • the complete nucleotide sequence of the 2.0kb PEL promoter, as it exists in the GUS reporter construct pAG142a, is shown in Figures 5A and B .
  • the 5' end of the 1.4 and 0.9kb truncations is also indicated in the figure.
  • the sequence of the PEL 2.0kb promoter is presented in Figures 3A and B and as SEQ ID NO:3.
  • the PEL 1.4kb and 0.9kb promoters correspond to nucleotides 564 to 2010 and 1099 to 2010, respectively, of the PEL 2.0kb promoter sequence presented as SEQ ID NO:3.
  • the 2.5kb PEL1 promoter fragment, described above was generated, truncated as PEL1 promoter fragments of 2.0, 1.4, and 0.9 kb, digested to produce the appropriate cohesive ends, and cloned into compatible sites in a reporter gene construct, comprised of the promoter translationally fused with GUS ( ⁇ -glucuronidase) and containing the nos terminator.
  • the resulting constructs comprising PEL1 promoter fragments of 2.0, 1.4, and 0.9 kb were named pAG142a-pel::GUS (2.0kb), pAG142b-pel::GUS (1.4kb) and pAG142c-pel::GUS (0.9kb), respectively.
  • the PEL1 fragments (2.0, 1.4 and 0.9 kb) correspond to nucleotides 1 to 2010, 564 to 2010 and 1099 to 2010, respectively, of SEQ ID NO:3.
  • Banana fruit was prepared for particle bombardment as described above.
  • the pAG142-pel::GUS (2.5kb); pAG142a-pel::GUS (2.0kb), pAG142b-pel::GUS (1.4kb), pAG142c-pel::GUS (0.9kb), pAG153-CsVMV::GUS, pAG159-TRX::GUS and pBI221-35S::GUS recombinant nucleic acid constructs were individually introduced into banana tissue by particle bombardment.
  • the relative activity of the banana fruit-associated promoter in the various constructs was determined by transient assay based on GUS reporter expression.
  • Figure 7 illustrates the results of GUS reporter assays, presented as the percent of banana fruit slices with GUS foci.
  • the primers, ACTIN 5'F (SEQ ID NO:30) and ACTIN 3'R (SEQ ID NO:31) span intron 3, which occurs at the 5' end of the resulting PCR product and have been effective amplify genDNA and cDNA templates from many different monocots and dicots, including apple, banana, cherry, grape, lettuce, maize, melon, pea, raspberry, tobacco, and tomato.
  • the genomic PCR fragment was slightly larger than the corresponding RT-PCR product, consistent with the presence of a small intron in the genomic fragment.
  • the melon genomic and RT-PCR fragments were sequenced and it was determined that the sequences were identical except for the presence of a single intron, corresponding to an intron formerly designated "intron 3".
  • the intron is 87 nt long and is not conserved between melon and other plant species.
  • oligonucleotide primers were synthesized that amplify a fragment upstream of the melon actin coding sequence.
  • the primers amplified a 1.6 kb fragment from the melon DraI promoter finder library. The fragment was cloned and sequenced.
  • the melon actin genomic fragment contains approximately 540 bp of 5' flanking sequence upstream of the translational start site and 1kb of transcribed sequence, which contains exons 1, 2, and a small portion of 3, and introns 1 and 2.
  • the transcriptional start site was estimated by amplifying and sequencing a 5' RACE fragment of the actin transcript from melon cDNA. Upstream elements with homology to functional motifs characterized in other plant actin promoters have also been identified.
  • Oligonucleotide primers used to amplify a melon actin gene fragment containing upstream regulatory regions included PF1 (SEQ ID NO:32), PF2 (SEQ ID NO:33), Actin PFb (SEQ ID NO:34), Actin PFc (SEQ ID NO:35) and MACTP int1 (SEQ ID NO:36).
  • the complete nucleotide sequence of the melon actin promoter, up to and including the translational start site, is presented in Figure 4 .
  • the transcriptional start site, as estimated by characterization of 5'RACE products, is indicated as + 1 in the sequence, placing the putative TATA-box at -47.
  • Features indicated as underlined in Figure 4 include the putative TATA-box at -47, nucleotides -251 to -205 in the melon actin promoter which is an A-rich region similar to the poly(dA-dT) region identified between nt positions -190 and -140 in the rice actin promoter.
  • the rice actin poly(dA-dT) was shown to act as a strong positive regulatory region for constitutive expression (Wang et al ., 1992). Nucleotides -185 to -146 constitute a region similar to the region between -150 and the TATA-box in the Arabidopsis ACT2 and ACT8 5' flanking sequences (An et al ., 1996). This region is highly conserved between the two Arabidopsis actin gene family members and may indicate the position of functional elements.
  • the underlined region from nucleotides -119 to -96 indicates a short direct repeat [4X(GCATTT)], a sequence motif that is present within an ORF of Sacchromyces cerevisiae and in non-coding regions of the Drosophila melanogaster and Arabidopsis thaliana genomes.
  • Motif (-84 to -51) is a region containing a dinucleotide repeat [18X(CT)] which motif is also present in the soybean Ac7 gene 5' flanking region.
  • CT dinucleotide repeat
  • the melon actin promoter sequence exhibits similarities to both the rice (model nionocot) and Arabidopsis (model dicot) strong constitutive actin promoters, and also to the soybean Ac7 actin gene 5' flanking sequence.
  • the melon actin promoter does not contain the putative root-associated expression element (CCCAA repeat) present in the rice actin promoter, and also contains unique sequence motifs.
  • CCAA repeat putative root-associated expression element
  • mACTIN The melon actin fragment amplified from genomic DNA up to the translational start site
  • Construct pAG167 contains the full-length (1.5kb) melon actin upstream genomic fragment cloned as a translational fusion with the uidA reporter gene encoding GUS.
  • the pAG167 GUS reporter gene construct is contained in a pUC vector.
  • the construct pAG4015 contains the full-length melon actin promoter operably linked (as a translational fusion) with the reporter gene encoding GUS, along with a selection cassette composed of the CsVMV promoter which controls expression of the nptII gene and confers kanamycin resistance. This construct is contained within the pPZP2000 binary vector.
  • pAG 167 The promoter activity of mACTIN was tested in banana embryogenic suspension cells using the construct designated "pAG 167" (mACTIN-GUS). Assays were performed at the Boyce Thompson Institute for Plant Research BTI (Ithaca, NY), where pAG167 was used to bombard embryogenic suspension cells of banana and relative GUS activity measured in protein extracts from the bombarded tissue as described below. The results of these assays indicated that level of GUS by pAG167 was comparable to that of the CaMV35S control.
  • Test plasmids used for bombardment included pAG167 (mACTIN-GUS) and control plasmids included pCaMV35S-GUS and pmaizeUbi-GUS, containing the uidA gene encoding GUS under the transcriptional control of the cauliflower mosaic virus 35S promoter and the maize ubiquitin promoter, respectively.
  • gold particles were coated with 2 ⁇ g of QIAGEN pure plasmid DNA of each test construct.
  • Six plates of GN cells were bombarded (10 ⁇ l Au:DNA mix, 800 psi) per construct. Six GN plates were kept aside as unbombarded negative controls.
  • mACTIN promoter was assayed for promoter activity in Allium spp. (garlic, Allium sativum and onion, Allium cepa ). Bombardment of onion and garlic target tissues with various reporter constructs was followed by histochemical GUS staining.
  • EtOH 75% EtOH was then added to cover the garlic or onion sample which is shaken gently each minute for 4 minutes, the EtOH is then drained off followed by the addition of sufficient 10% bleach/2 drops Tween 20/1000 ml to cover the samples followed by intermittent shaking for 10 minutes. The bleach was then drained off. the samples rinsed 3 times with sterile diH 2 O and once with sterile 500 ml diH 2 O/2 ml PPM mix (Plant Preservative Mixture. Plant Cell Technology, Washington, DC). The samples were cut and bombard on the same day.
  • the sterilization procedure specific to in vivo leaves of scallion included the steps of agitating the leaves gently in 70% EtOH for 30 seconds, draining off the EtOH, agitating the leaves gently in 10% bleach with Tween20 for 1 minute, draining off the bleach, rinsing 3 times with sterile water, and rinsing 1 time with 2 ml PPM in 500 ml sterile water. This was followed by cutting the leaves into segments and plating them abaxial side up (exterior side up) on PAC 1 medium. The samples were cut and bombard on the same day.
  • the types of garlic tissue tested included: (1) the exterior of a garlic clove, cut in half longitudinally; (2) a cross sectional slice of clove; and (3) the interior of a garlic clove, cut in half longitudinally. 14-22 pieces of garlic were bombarded for each construct tested except pAG167 (mACTIN) for which only 6 pieces were bombarded.
  • Particle bombardment was carried out using a PDS 1000/He microprojectile gun (Bio-Rad) and gold particles, as described above for banana.
  • plasmid constructs containing the GUS gene under transcriptional control of various promoters were evaluated including: pAG138m-RE4::GUS, pAG147-promoterless GUS (which contains the GUS gene without regulatory elements, and serves as a negative control), pAG153-CsVMV::GUS (which contains the CsVMV promoter and serves as a positive control), pAG167-mACTIN::GUS and PBI221-35S::GUS (which contains the CaMV promoter and serves as a positive control). (See Example 3.)
  • pAG153 (CsVMV) and pAG167 (mACTIN) demonstrated stronger expression of GUS than the CaMV 35S promoter (pBI221) in garlic cloves and onion bulbs.
  • GUS expression under the control of pAG153 (CsVMV) and pAG167 (mACTIN) was similar to that of the CaMV 35S promoter (pBI221).
  • the mACTIN promoter was also tested for activity in a model dicot ( Arabidopsis thaliana ) after transformation with a nucleic acid construct containing the reporter gene encoding GUS under the control of the mACTIN promoter.
  • Construct pAG4015 contains two expression cassettes: adjacent to the left T-DNA border is found the selection cassette contains the nptII gene conferring kanamycin resistance under the control of the CsVMV promoter and the G7 terminator; and adjacent to the right T-DNA border is found the GUS reporter gene under the control of the mACTIN promoter and the nos terminator.
  • Arabidopsis thaliana (Col-0 ecotype) plants were grown in soil under long day conditions (16h of light). The primary inflorescences were trimmed from the plants to encourage growth of lateral inflorescence, and plants were transformed 6 days after the trimming.
  • the Agrobacterium strain GV3101 containing helper plasmid pMP90RK was transformed with pAG4015 by electroporation. The plants were transformed following the in planta transformation method described by Clough and Bent, Plant Journal 16:735-743, 1998 . Briefly, the Agrobacterium culture containing pAG4015 was grown to an OD 600 of 1.5 to 2.5.
  • the cells were harvested by centrifugation and resuspended to an OD 600 of approximately 0.80 in submersion media containing 5% sucrose, 0.04% Silwet L-77, 10 mM M 2 Cl and 44 nM 6-Benzylaminopurine.
  • the plants were inverted into the cell suspension for 15 minutes, then the plants were then placed on their sides under a dome for 16-24 hours to maintain high humidity.
  • the plants were grown for 5 weeks until the siliques were brown and dry.
  • T1 seed was harvested from the plants, surface sterilized and germinated on plates containing 1/2 MS medium, 0.7% Agar and 50 ⁇ g/ml kanamycin monosulfate. Transformed seedlings were identified as those resistant to the kanamycin monosulate.
  • Figs. 11A-D The results of staining for GUS reporter gene activity in Arabidopsis stably transformed with the construct pAG4015, presented in Figs. 11A-D indicate that the mACTIN promoter directs strong reporter gene expression in seedlings as determined by histochemical staining, with GUS staining especially apparent in roots (Fig. 11B). After the formation of the rosette, more intense blue staining was apparent in the cotyledons, early true leaves and roots than in the later developing leaves (Fig. 11C). In mature leaves, the mACTIN promoter is also active, with strong histochemical staining in leaves as well as flowers (Fig 11D).
  • Two modified form of the banana fruit-specific TRX promoter were constructed by (1) adding a monocot intron to the 3' end of the banana TRX promoter and (2) by fusing the banana TRX promoter with the melon actin promoter at the TATA-box.
  • the first modification to the TRX promoter involved the addition of a DNA fragment containing intron 3 from the maize 02 gene to the Ncol site engineered into the 3' end of the banana fruit-specific TRX promoter.
  • the complete nucleotide sequence of the maize O2 gene was obtained from GenBank Accession X15544, within which intron 3 is between nucleotides 3020 to 3105.
  • the maize 02 intron 3 is a typical monocot intron: it is short, only 83 nt ; A+U-rich (60%); and contains appropriate consensus splice sites. Oligonucleotides were designed to amplify the maize 02 intron 3 and then subclone it into the NcoI site at the 3' end of the TRX promoter.
  • the oligonucleotide primers used to amplify the maize 02 intron are listed below.
  • the amplification product containing the 02 intron was cloned into an intermediate vector, sequenced to confirm its identity, then subcloned in the correct orientation into the NcoI site engineered into the 3' end of the TRX promoter.
  • After the addition of the intron there are two potential ATG start codons associated with any linked gene, one at each end of the intron.
  • the construct was designed such that if the added 02 intron is properly spliced, the upstream ATG in the resulting transcript is in-frame with the downstream ATG.
  • the resulting fusion protein will contain four additional amino acids (MEKA) at the N-terminus. If the intron is not properly spliced, the upstream ATG will not be in-frame with the linked gene, but translation can still be initiated from the downstream ATG. In this case, the resulting protein will not contain any additional amino acids.
  • the O2 intron-modified TRX promoter fused to the GUS reporter gene was designated pAG759. The complete nucleotide sequence of the TRX-O2 intron fusion promoter appears in Figures 5A-B (SEQ ID NO:5).
  • O2int_F SEQ ID NO:37
  • O2int_R SEQ ID NO:38
  • oligonucleotides used to amplify intron 3 of the maize O2 gene for subcloning into the NcoI site at the 3' end of the banana TRX promoter are presented below with the Ncol site engineered into the sequence for subcloning indicated as underlined in Table 5.
  • the banana TRX promoter was fused to the melon actin promoter at the TATA-box, resulting in a fusion promoter having the sequence presented as SEQ ID NO:6.
  • Both promoters contained an identical, canonical plant TATA-box (TATAAA), which was used to perform a perfect fusion between them at that site.
  • Chimeric oligonucleotide primers (shown below) were designed that were complementary to both of the promoter sequences.
  • a fragment containing the banana TRX promoter from the 5' end to the TATA box was amplified from pAG159 using 1233 (SEQ ID NO:42) and (Act)TRX_R (SEQ ID NO:40).
  • the product was approximately 0.8kb.
  • the melon actin fragment for fusion to the Thi promoter fragment was amplified from pAG167 using GUS5'R (SEQ ID NO:41) and (TRX)Act_F (SEQ ID NO:39) and a PE480 thermal cycler: 25 cycles (94°C, 30 seconds: 60°C. 30 seconds; 72°C, 90 seconds), 1 cycle (72°C, 10min).
  • the 1.2kb fragment from the melon actin promoter contained the transcription start site, 5' untranslated region intron, and the translational start site that had been engineered to contain an Ncol site for ease of subcloning linked genes.
  • the fragments contained a complementary overlapping region of 21 nucleotides, including the TATA-box.
  • the two fragments were fused by combining them in a second amplification reaction and using the end primers (1233 and GUS5'R) for amplification and a PE480 thermal cycler: 25 cycles (94°C, 30 seconds; 60°C, 30 seconds; 72 °C, 150 seconds), 1 cycle (72°C for 10 min).
  • the resulting reaction products were separated on an agarose gel, and the fragment of the correct predicted size was gel purified, digested with HinDIII and NcoI, ligated into a vector containing the GUS reporter gene and given the designation pAG749.
  • Oligonucleotide primers used to amplify and assemble the TRX-melon actin fusion promoter included (TRX)Act_F (SEQ ID NO:39), (Act)TRX_R (SEQ ID NO:40), GUS5'R (SEQ ID NO:41) and 1233 (SEQ ID NO:42).
  • the modified TRX promoters were cloned into expression constructs (as a translational fusion) with the reporter gene encoding GUS, resulting in constructs designated pAG749 (TRX-actin::GUS) and pAG759 (TRX-intron::GUS).
  • the modified TRX promoters were tested for GUS expression in the banana fruit slice transient expression assay described above.
  • the samples used were either green, non-ethylene-treated fruit (green), green fruit but within 24h of ethylene treatment (PCI 1), yellow fruit with green tips (PCI 4) or leaf.
  • the relative activity of the TRX-intron, TRX-actin fruit-associated fusion promoters and the CsVMV viral promoter in promoting GUS expression is expressed as both percent of fruit slices showing foci after histochemical staining ( Fig. 12A ) and mean number of foci per fruit slice ( Fig. 12B ), in banana fruit slices.
  • the strong constitutive CsVMV promoter was used as a positive control.
  • the TRX-intron and TRX-actin modifications have improved performance relative to the banana fruit-specific TRX promoter.
  • the TRX-actin fusion promoter displays transient expression activity approximately equal to the strong constitutive promoter CsVMV. whereas the TRX-intron fusion is slightly less active on average. Furthermore, the TRX-intron and TRX-actin promoters have lower activity in banana leaves, indicating that the promoters have retained the tissue specificity of the TRX promoter. Table 4. Banana And Melon Actin Promoter-Containing Nucleic Acid Constructs .
  • 1 Figure 2 The modified TRX promoter sequence, which corresponds to . nucleotides 13 - 990 of the sequence presented in Figure 1 , with the exception that restriction sites for BamHI and NcoI have been engineered into the sequence in Figure 2 . at the extreme 5' and 3' ends, respectively.
  • 2 Figure 3A-B Complete sequence of the PEL1 2.0kb promoter.
  • FIG. 4 the complete nucleotide sequence of the melon actin promoter as it exists in constructs pAG167 and pAG4015 (“mACTIN”).
  • Figures 5A-B the complete nucleotide sequence of the banana fruit specific promoter containing intron 3 from the maize 02 gene engineered into the 3' end of the banana fruit-specific TRX promoter ("TRX-INTRON")
  • Figure 6 the complete nucleotide sequence of the banana fruit specific promoter TRX fused to the melon actin promoter downstream of the TATA-box (“TRX-ACTIN").

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